ORPHA:404469
Rare female infertility due to oocyte maturation defect
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare female infertility due to oocyte maturation defect | |
| fr | Infertilité féminine rare due à un défaut de maturation de l'ovocyte | Infertilité féminine rare due à un défaut de maturation ovocytaire |
| de | Seltene weibliche Infertilität durch Störung der Oozytenreifung | |
| es | Infertilidad femenina rara por un defecto de maduración de los ovocitos | |
| it | Infertilità femminile da difetto di fecondazione | |
| nl | Zeldzame vrouwelijke onvruchtbaarheid door defect van oöcytmaturatie | |
| pt | Infertilidade feminina por defeito de fertilização | |
| pl | Niepłodność żeńska z powodu wady zapłodnienia | |
| cs | Ženská neplodnost způsobená poruchami fertilizace | Ženská neplodnost způsobená poruchami oplodnění |
| uk | Рідкісне жіноче безпліддя, зумовлене дефектом дозрівання яйцеклітин | |
| zh | 卵母细胞成熟缺陷导致的罕见女性不育 | |
| tr | Oosit olgunlaşma defektine bağlı nadir kadın infertilitesi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18444 | E | validated | |
| UMLS | C5681140 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:98049Rare female infertility
rare infertility disorders - ORPHA:400008Rare genetic female infertility
rare genetic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/404469
- This record as JSON: /data/d/404469.json